Intrinsic curvature in duplex DNA inhibits human Topoisomerase I
Human Topoisomerase I (hTopo I) have been known as a potential target for cancer therapy. A series of duplex DNA with different intrinsic curvatures have been designed as inhibitors to hTopo I. The activities of hTopo I on relaxing supercoiled plasmid pUC 19 are apparently diminished in the presence...
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sg-ntu-dr.10356-990112020-03-07T12:34:45Z Intrinsic curvature in duplex DNA inhibits human Topoisomerase I Yang, Zhaoqi Li, Dawei Guo, Juanjuan Shao, Fangwei Li, Tianhu School of Physical and Mathematical Sciences Human Topoisomerase I (hTopo I) have been known as a potential target for cancer therapy. A series of duplex DNA with different intrinsic curvatures have been designed as inhibitors to hTopo I. The activities of hTopo I on relaxing supercoiled plasmid pUC 19 are apparently diminished in the presence of the curved DNA. More potent inhibitions and smaller IC50 are achieved by duplex DNA with higher curvatures. EMSA indicates that hTopo I can recognize the curved DNA through binding interactions. Our studies demonstrate that the activity of hTopo I can be modulated by the intrinsic curvature of linear DNA and provide a new avenue to design curved DNA as hTopo I inhibitors with high therapeutic efficiency and low toxicity. 2013-08-01T04:22:22Z 2019-12-06T20:02:18Z 2013-08-01T04:22:22Z 2019-12-06T20:02:18Z 2012 2012 Journal Article Yang, Z., Li, D., Guo, J., Shao, F.,& Li, T. (2012). Intrinsic curvature in duplex DNA inhibits Human Topoisomerase I. Bioorganic & Medicinal Chemistry Letters, 22(3), 1322-1325. 0960-894X https://hdl.handle.net/10356/99011 http://hdl.handle.net/10220/12779 10.1016/j.bmcl.2011.12.089 en Bioorganic & medicinal chemistry letters |
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Human Topoisomerase I (hTopo I) have been known as a potential target for cancer therapy. A series of duplex DNA with different intrinsic curvatures have been designed as inhibitors to hTopo I. The activities of hTopo I on relaxing supercoiled plasmid pUC 19 are apparently diminished in the presence of the curved DNA. More potent inhibitions and smaller IC50 are achieved by duplex DNA with higher curvatures. EMSA indicates that hTopo I can recognize the curved DNA through binding interactions. Our studies demonstrate that the activity of hTopo I can be modulated by the intrinsic curvature of linear DNA and provide a new avenue to design curved DNA as hTopo I inhibitors with high therapeutic efficiency and low toxicity. |
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School of Physical and Mathematical Sciences |
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School of Physical and Mathematical Sciences Yang, Zhaoqi Li, Dawei Guo, Juanjuan Shao, Fangwei Li, Tianhu |
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Yang, Zhaoqi Li, Dawei Guo, Juanjuan Shao, Fangwei Li, Tianhu |
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Yang, Zhaoqi Li, Dawei Guo, Juanjuan Shao, Fangwei Li, Tianhu Intrinsic curvature in duplex DNA inhibits human Topoisomerase I |
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Yang, Zhaoqi |
title |
Intrinsic curvature in duplex DNA inhibits human Topoisomerase I |
title_short |
Intrinsic curvature in duplex DNA inhibits human Topoisomerase I |
title_full |
Intrinsic curvature in duplex DNA inhibits human Topoisomerase I |
title_fullStr |
Intrinsic curvature in duplex DNA inhibits human Topoisomerase I |
title_full_unstemmed |
Intrinsic curvature in duplex DNA inhibits human Topoisomerase I |
title_sort |
intrinsic curvature in duplex dna inhibits human topoisomerase i |
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2013 |
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https://hdl.handle.net/10356/99011 http://hdl.handle.net/10220/12779 |
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